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A Method for Mining Infrequent Causal Associations and Its Application in Finding Adverse Drug Reaction Signal Pairs

机译:一种罕见因果关联的挖掘方法及其在药物不良反应信号对中的应用

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In many real-world applications, it is important to mine causal relationships where an event or event pattern causes certain outcomes with low probability. Discovering this kind of causal relationships can help us prevent or correct negative outcomes caused by their antecedents. In this paper, we propose an innovative data mining framework and apply it to mine potential causal associations in electronic patient data sets where the drug-related events of interest occur infrequently. Specifically, we created a novel interestingness measure, exclusive causal-leverage, based on a computational, fuzzy recognition-primed decision (RPD) model that we previously developed. On the basis of this new measure, a data mining algorithm was developed to mine the causal relationship between drugs and their associated adverse drug reactions (ADRs). The algorithm was tested on real patient data retrieved from the Veterans Affairs Medical Center in Detroit, Michigan. The retrieved data included 16,206 patients (15,605 male, 601 female). The exclusive causal-leverage was employed to rank the potential causal associations between each of the three selected drugs (i.e., enalapril, pravastatin, and rosuvastatin) and 3,954 recorded symptoms, each of which corresponded to a potential ADR. The top 10 drug-symptom pairs for each drug were evaluated by the physicians on our project team. The numbers of symptoms considered as likely real ADRs for enalapril, pravastatin, and rosuvastatin were 8, 7, and 6, respectively. These preliminary results indicate the usefulness of our method in finding potential ADR signal pairs for further analysis (e.g., epidemiology study) and investigation (e.g., case review) by drug safety professionals.
机译:在许多实际应用中,重要的是要挖掘因果关系,其中事件或事件模式导致某些结果发生的可能性很小。发现这种因果关系可以帮助我们预防或纠正由其前因引起的负面结果。在本文中,我们提出了一种创新的数据挖掘框架,并将其应用于挖掘电子患者数据集中潜在的因果关系,而这些事件中与药物相关的事件很少发生。具体来说,我们基于先前开发的计算性,模糊识别主导决策(RPD)模型,创建了一种新颖的兴趣度度量,即因果杠杆效应。在此新措施的基础上,开发了一种数据挖掘算法来挖掘药物及其相关药物不良反应(ADR)之间的因果关系。该算法在从密歇根州底特律的退伍军人事务医疗中心获取的真实患者数据上进行了测试。检索到的数据包括16,206名患者(15,605例男性,601例女性)。独家因果关系杠杆作用用于对三种选定药物(即依那普利,普伐他汀和罗苏伐他汀)中每种药物之间的潜在因果关系进行排名,并记录了3,954个记录的症状,每种症状均对应于潜在的ADR。由我们项目小组的医生评估了每种药物的前10个药物症状对。依那普利,普伐他汀和瑞舒伐他汀被认为可能是真正的ADR的症状数分别为8、7和6。这些初步结果表明,我们的方法在寻找潜在的ADR信号对以进行进一步分析(例如流行病学研究)和由药物安全专业人员进行调查(例如病例复查)中非常有用。

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